Allele Registry

Canonical Allele Identifier: PA120705

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010487

RCV000640478

RCV001269612

ClinVar Variation:

9813

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Ala65Thr	CA120703 NM_001011645.3:c.193G>A